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2,5-Dichloro-N-methoxy-N-methylisonicotinamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

864674-17-9

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864674-17-9 Usage

Class of organic compounds

pyridinecarboxamides
Used as an intermediate in the synthesis of other chemical compounds
Potential applications in pharmaceutical and agrochemical industries
Studied for potential antitubercular and antifungal activities
Should be handled with care
Harmful if ingested or inhaled
May cause skin and eye irritation upon contact

Check Digit Verification of cas no

The CAS Registry Mumber 864674-17-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,4,6,7 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 864674-17:
(8*8)+(7*6)+(6*4)+(5*6)+(4*7)+(3*4)+(2*1)+(1*7)=209
209 % 10 = 9
So 864674-17-9 is a valid CAS Registry Number.

864674-17-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-dichloro-N-methoxy-N-methylpyridine-4-carboxamide

1.2 Other means of identification

Product number -
Other names 2,5-DICHLORO-N-METHOXY-N-METHYLISONICOTINAMIDE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:864674-17-9 SDS

864674-17-9Downstream Products

864674-17-9Relevant academic research and scientific papers

Casein kinase 1 (CK1) inhibitor for plants (by machine translation)

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Paragraph 0053; 0104-0107, (2020/02/14)

[Problem] to provide various lead compounds PHA derivatives, and/or circadian rhythm control agent having stronger CK1 inhibitor activity. [Solution] a compound represented by formula I, or a salt thereof or a solvate thereof. (R1 The, H or C1 - 5 A straight-chain, branched or cyclic alkyl group, alkenyl group or alkynyl group, R2 The, H, halogen (F, Cl, Br or I), or a C1 - 4 The alkyl group, the ring A, 5 - 8 membered lactam ring showing; however, R1 And R2 Except H together. )[Drawing] no (by machine translation)

2-PYRIDINYL[7-(SUBSTITUTED-PYRIDIN-4-YL) PYRAZOLO[1,5-A]PYRIMIDIN-3-YL]METHANONES

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Page/Page column 45, (2010/02/14)

The present invention provides novel 2-pyridinyl[7(pyridin-4-yl)pyrazolo[1,5--a]pyrimidin-3-yl]methanones with at least one substituent on the 4-pyridinyl ring having the chemical structure of formula (I): The invention further provides compositions and methods employing the novel 2-pyridinyl[7-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidin-3-yl]methanones of formula: (I) in to modulate GABA and GABA receptor physiology to elicit therapeutic responses in mammalian subjects to alleviate neurological or psychiatric disorders, including stroke, head trauma, epilepsy, pain, migraine, mood disorders, anxiety, post traumatic stress disorder, obsessive compulsive disorders, mania, bipolar disorders, schizophrenia, seizures, convulsions, tinnitus, neurodegenerative disorders including Alzheimer's disease, amyotrophic lateral sclerosis and Parkinson's disease, Huntington's chorea, depression, bipolar disorders, mania, trigeminal and other neuralgia, neuropathic pain, hypertension, cerebral ischemia, cardiac arrhythmia, myotonia, substance abuse, myoclonus, essential tremor, dyskinesia and other movement disorders, neonatal cerebral hemorrhage, and spasticity, as well as other psychiatric and neurological disorders mediated by GABA and/or GABA receptors.

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